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SIRT1与PARP-1在响应DNA损伤时的功能相互作用对AIF介导的细胞死亡的调控

Control of AIF-mediated cell death by the functional interplay of SIRT1 and PARP-1 in response to DNA damage.

作者信息

Kolthur-Seetharam Ullas, Dantzer Françoise, McBurney Michael W, de Murcia Gilbert, Sassone-Corsi Paolo

机构信息

Institut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS, Inserm, Université Louis Pasteur, Strasbourg, France.

出版信息

Cell Cycle. 2006 Apr;5(8):873-7. doi: 10.4161/cc.5.8.2690. Epub 2006 Apr 17.

Abstract

Cell survival after genotoxic stress is determined by a counterbalance of pro- and anti-death factors. Sirtuins (SIRTs) are deacetylases that promote cell survival whereas poly(ADP-ribose) polymerases (PARPs) can act both as survival and death inducing factor and the two protein families are strictly dependent on NAD(+) for their activities. Here we report that SIRT1 modulates PARP-1 activity upon DNA damage. Activation of SIRT1 by resveratrol leads to reduced PARP-1 activity and there is a drastic increase in PAR synthesis in sirt1-null cells. The unbalanced regulation of PARP-1 in the absence of SIRT1 results in AIF (apoptosis inducing factor)-mediated cell death. Our findings establish a functional link between the two NAD+-dependent enzyme systems and provide a physiological interpretation for the mechanism of death in cells lacking SIRT1.

摘要

基因毒性应激后的细胞存活取决于促死亡因子和抗死亡因子之间的平衡。沉默调节蛋白(SIRTs)是促进细胞存活的去乙酰化酶,而聚(ADP-核糖)聚合酶(PARPs)既可以作为存活诱导因子,也可以作为死亡诱导因子,这两个蛋白家族的活性都严格依赖于NAD(+)。在此我们报告,SIRT1在DNA损伤时调节PARP-1的活性。白藜芦醇激活SIRT1会导致PARP-1活性降低,而在sirt1基因缺失的细胞中PAR合成会急剧增加。在缺乏SIRT1的情况下,PARP-1的失衡调节会导致凋亡诱导因子(AIF)介导的细胞死亡。我们的研究结果在这两个依赖NAD+的酶系统之间建立了功能联系,并为缺乏SIRT1的细胞中的死亡机制提供了生理学解释。

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